First Report of Tobacco Streak Ilarvirus from Honeysuckle

A honeysuckle (Lonicera fragrantissima) shrub on the grounds of the former Plant Quarantine Station, Glenn Dale, MD, had chlorotic leaves on some shoot tips and a mild veinal chlorosis. Young leaves were triturated in buffer and rub-inoculated onto a series of potential indicator hosts. The virus incited necrotic local lesions and necrosis of the growing point in Chenopodium quinoa, etched ringspots on inoculated leaves of Nicotiana tabacum Xanthi nc, mosaic in Zinnia violacea, and chlorotic local lesions in Tetragonia tetragonioides. It did not infect any of 46 other herbaceous genera in families Cucurbitaceae, Fabaceae, Asteraceae, Solanaceae, or Brassicaceae. In gel diffusion tests with symptomatic leaves from tobacco, this virus reacted with antiserum to tobacco streak virus (TSV) HR strain, but did not react with antisera to alfalfa mosaic or with antisera to 12 viruses in the NEPO or Sobemovirus groups. Virus in leaves directly from the source shrubs, tested by enzyme-linked immunosorbent assay (ELISA), also reacted with TSV strain HF antiserum. Examination by electron microscopy of leaf dips revealed isometric particles 27 nm in diameter. The now 12-ft tall shrubs were grown from seed imported from China in 1914 (PI 40689). This species is now widely commercially available in the U.S. and grown for its fragrant late winter flowers (2). Viral-infected Lonicera spp. have been reported from Europe, Russia, Japan, and Canada (1). TSV is reported to be seed-borne in several other genera. Among other viruses reported from honeysuckle are Lonicera latent carlavirus, tobacco leaf curl geminivirus, alfalfa mosaic virus, tomato bushy stunt virus, a rhabdovirus, and an aphid transmitted virus. References: (1) R. W. Fulton. CMI/AAB Descriptions of Plant Viruses No. 307, 1985. (2) C. J. Perkin. Plantsman 12:215, 1991.

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A New Ilarvirus Isolated from Grapevine in Greece

Plant Disease ◽

10.1094/pdis.2000.84.12.1345c ◽

2000 ◽

Vol 84 (12) ◽

pp. 1345-1345 ◽

Cited By ~ 2

Author(s):

S. M. Girgis ◽

F. Bem ◽

P. E. Kyriakopoulou ◽

C. I. Dovas ◽

A. P. Sklavounos ◽

...

Keyword(s):

Sequence Data ◽

Sequence Similarity ◽

Infected Plant ◽

Chenopodium Quinoa ◽

Tobacco Streak Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Streak Virus ◽

Degenerate Primers ◽

Severe Stunting ◽

Local Lesions

In 1994, characteristic viruslike symptoms on grapevine were reported in the collection of the Grapevine Institute in Athens, Greece, on the hybrid Baresana × Baresana. The symptoms were sharp angular mosaic, leaf crinkle, and little leaf. The affected vines showed gradual decline and severe stunting or death. Such vines produced abortive flowers or very few berries with smaller, wrinkled, and nongerminating seeds. Serological testing, by enzyme-linked immunosorbent assay (ELISA), of the affected vines against the most common grapevine viruses Alfalfa mosaic, Arabis mosaic, Grapevine fanleaf, Grapevine fleck, Grapevine A, Rasberry ringspot, and grapevine leafroll-associated viruses gave negative results. A virus was isolated from affected grapevine young leaves by mechanical inoculation of Gomphrena globosa and single lesioned. The virus host range included G. globosa (local and systemic dark red or necrotic lesions), Chenopodium quinoa (necrotic local lesions and systemic mottle), and three tobacco cultivars (sharp necrotic local lesions, 1 to 3 mm in diameter). Pollination of C. quinoa with pollen from infected plant gave about 30% infected seedlings. The virus was purified from C. quinoa by differential centrifugation using 0.02 M phosphate buffer pH 8.0, containing 0.01 M DIECA and 0.01 M sodium thioglycolate as extraction buffers. In a purified preparation, quasisphaerical virus particles of about 29 nm were observed. Electrophoretic mobility of the viral coat protein showed a molecular weight of 30 kDa. Using purified preparations, an antiserum was obtained with a titer of 1:1024 in microprecipitin test and an optimum IgG dilution in ELISA of 1:10,000 for maximum absorption at OD405 nm Using degenerate primers designed from homologous regions in RNA-2 corresponding to a fragment of the polymerase gene of Ilarviruses, the expected 381-bp polymerase chain reaction product was obtained. This product was cloned and sequenced. Comparisons with sequence data from the homologous regions of RNA-2 of other known Ilarviruses, showed that the sequence of the above 381-bp amplicon shared 72% sequence similarity with Tobacco streak virus, 67% of Citrus variegation virus and Spinach latent virus, 66% of Asparagus virus 2 and Elm mottle virus, and 65% of Citrus leaf rugose virus. Based on the above data, it is concluded that the isolated virus is an Ilarvirus with closest similarity to Tobacco streak virus. From the relative bibliography (1–3) it appears that the virus reported here is different from Grapevine line pattern virus, a possible Ilarvirus, previously reported from Hungary. References: (1) J. Lehoczky et al. Kertgazdasag 19:61, 1987. (2) J. Lehoczky et al. Phytoparasitica 17:59, 1989. (3) J. Lehoczky et al. Phytopathol. Medit. 31:115, 1992.

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Fruit Distortion Mosaic Disease of Okra in India

Plant Disease ◽

10.1094/pdis.2003.87.11.1395a ◽

2003 ◽

Vol 87 (11) ◽

pp. 1395-1395 ◽

Cited By ~ 10

Author(s):

M. Krishnareddy ◽

Salil Jalali ◽

D. K. Samuel

Keyword(s):

Electron Microscopy ◽

Mosaic Virus ◽

Tamil Nadu ◽

Plant Viruses ◽

Mosaic Disease ◽

Tobacco Streak Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Streak Virus ◽

Field Samples ◽

Local Lesions

Okra (Abelmoscus esculentus (L.) Moench) is an important vegetable crop of India and other subropical and tropical countries. In 2000 and 2001, in the states of Karnataka and Tamil Nadu, okra was severely affected by a new disease. Since that time, the disease has spread to other states: Andhra Pradesh, Madhya Pradesh, Haryana, and Maharashtra. Chlorotic spots, chlorotic leaf blotches, distortion of leaves, chlorotic streaking, distortion of fruits, and severe yield losses as much as 63% characterize the disease. The causal virus induces local and systemic chlorotic and necrotic lesions on Vigna unguiculata (L.) Walp. cv. C-152 and Chenopodium amaranticolor Coste & Reyne., chlorotic local lesions and mosaic on Cucumis sativus L., necrotic local lesions on Gossypium hirsutum L. and black gram (Vigna mungo L.), and chlorotic local lesions and systemic necrosis on sunflower (Helianthus annuus L.). Host reactions on these species are similar to those described for the ilarvirus Tobacco streak virus (TSV) (3). Electron microscopic observation of leafdip preparations from field samples and partially purified virus preparations revealed the presence of isometric virus particles measuring 25 to 30 nm in diameter. The virus was purified from mechanically inoculated okra by differential and sucrose density gradient centrifugation, and disease symptoms were reproduced in okra mechanically inoculated with the purified virus. In direct antigen coated enzyme-linked immunosorbent assay and immunosorbent electron microscopy tests, the purified virus and sap extracts reacted positively with polyclonal antibodies to TSV, the ilarvirus associated with sunflower necrosis and peanut stem necrosis diseases (1,2), but did not react positively to Turnip mosaic virus and Okra mosaic virus that are previously reported to infect okra. In reverse transcription-polymerase chain reaction (RT-PCR), using oligonucleotide primers designed to amplify the entire coat protein region of TSV, an approximately 800-bp DNA fragment was obtained from purified virus and okra displaying fruit distortion mosaic disease (OFDM) but not from healthy okra. On the basis of host range, serological relationship, electron microscopy, and RTPCR amplification, the virus causing OFDM is an ilarvirus closely related to TSV. To our knowledge, this is the first report of the occurrence of an ilarvirus in okra, and is the third and most recent report of an ilarvirus related to TSV causing disease in crops on the Indian subcontinent (1,2). References:(1). A. I. Bhat et al. Arch. Virol. 147:651, 2002. (2). A. S. Reddy et al. Plant Dis. 86:173, 2002. (3). S. W. Scott. Tobacco streak virus. No 381 in: Descriptions of Plant Viruses. CMI/AAB, Surrey, U.K., 2001.

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Strawberry latent ringspot virus Infecting Roses in India

Plant Disease ◽

10.1094/pdis.2004.88.1.86c ◽

2004 ◽

Vol 88 (1) ◽

pp. 86-86 ◽

Cited By ~ 5

Author(s):

S. Kulshrestha ◽

V. Hallan ◽

G. Raikhy ◽

R. Ram ◽

A. A. Zaidi

Keyword(s):

Plant Viruses ◽

Ringspot Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Chain Reaction ◽

Specific Primers ◽

Chenopodium Amaranticolor ◽

Elisa Kit ◽

Local Lesions ◽

Young Leaves ◽

Polymerase Chain

Rose is an economically important crop of India and the world. A survey of rose plantations in and near the Kangra Valley of Himachal Pradesh, India, showed virus-like symptoms, including yellow flecking in young leaves and reduction in leaflet size, while some were symptomless. These symptoms are similar to those for Strawberry latent ringspot virus (SLRSV) (1). Sap inoculation from symptomatic and some symptomless leaves to Chenopodium amaranticolor resulted in chlorotic local lesions followed by systemic chlorosis. SLRSV was detected in this indicator host and six rose cultivars (Happiness, Iceberg, First Prize, Ganga, Pink Panther, and Oklahoma) showing characteristic symptoms of SLRSV using enzyme-linked immunosorbent assay (ELISA) with ELISA kit (DSMZ, Braunschweig, Germany). Reverse transcription-polymerase chain reaction was performed with SLRSV-specific primers (2), and a product of the expected size of ˜181 bp was amplified. The authenticity of the fragment was confirmed by sequencing. Isolated SLRSV was also inoculated to seed-grown rose seedlings and after 20 days postinoculation the same symptoms (yellow flecking in young leaves) were observed. These results established the identity of the virus that caused yellow flecking on rose leaves in India as SLRSV. To our knowledge, this is the first report of SLRSV infecting rose in India. References: (1) A. F. Murant. Strawberry latent ringspot virus. No. 126 in: Description of Plant Viruses, CMI/AAB, Surrey, U.K., 1974. (2) E. Bertolini et al. J. Virol. Methods 96:33, 2001.

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First Report of Parietaria mottle virus on Tomato in Spain

Plant Disease ◽

10.1094/pdis.2001.85.11.1210c ◽

2001 ◽

Vol 85 (11) ◽

pp. 1210-1210 ◽

Cited By ~ 18

Author(s):

J. Aramburu

Keyword(s):

Mosaic Virus ◽

Polyclonal Antiserum ◽

Mottle Virus ◽

Tomato Mosaic Virus ◽

Tobacco Streak Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Streak Virus ◽

Range Data ◽

Local Lesions ◽

Plant Pathol

During spring 2001, plants of different tomato (Lycopersicon esculentum) cultivars grown in several commercial fields in the eastern Catalonia Region of Spain had fruit with brown patches and young leaves with rings and a bright necrotic mosaic that progressed to stem necrosis of the apex, which might die and later develop new symptomless shoots. The symptoms were similar to those of Cucumber mosaic virus (CMV) and Tomato spotted wilt virus (TSWV). Sap of tomato sample R1 (in buffered saline [0.02 M sodium phosphate, 0.15 M NaCl at pH 7.2, containing 0.2% 2-mercaptoethanol]) was infective to Cucumis sativus (local necrosis), tomato cv. Marmande (systemic infection consisting of chlorotic local lesions and necrotic mosaic), Nicotiana clevelandii and N. benthamiana (chlorosis and rosetting), and Chenopodium quinoa (chlorotic local lesions, systemic mottle, and leaf distortion). The sap was not infective to N. glutinosa, N. tabacum cv. Xanthi, Datura stramonium, or Gomphrena globosa. The host range data indicated that the infective agent in sample R1 could be Parietaria mottle virus (PMoV) (1). Symptomatic plants inoculated in a greenhouse with the R1 isolate and symptomatic from tomato plants from the field were analyzed by indirect enzyme-linked immunosorbent assay (ELISA) and had minimum ELISA values at least 10-fold higher than healthy controls, using a polyclonal antiserum (provided by P. Roggero) of a tomato strain of PMoV denoted tomato virus 1 (2). The R1 isolate of PMoV was negative in ELISA when analyzed with commercial antisera to TSWV, CMV, Tomato mosaic virus, Tomato bushy stunt virus, Potato Y virus, Tobacco etch virus, Pelargonium zonate spot virus, and Tobacco streak virus. References: (1) P. Caciagli et al. Plant Pathol. 38:577, 1989. (2) P. Roggero et al. J. Plant Pathol. 82:159, 2000.

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Assessment of Common Soybean-Infecting Viruses in Ohio, USA, Through Multi-site Sampling and High-Throughput Sequencing

Plant Health Progress ◽

10.1094/php-rs-16-0018 ◽

2016 ◽

Vol 17 (2) ◽

pp. 133-140 ◽

Cited By ~ 1

Author(s):

Junping Han ◽

Leslie L. Domier ◽

Bryan J. Cassone ◽

Anne Dorrance ◽

Feng Qu

Keyword(s):

Mosaic Virus ◽

High Throughput ◽

High Throughput Sequencing ◽

Virus Disease ◽

Soybean Mosaic Virus ◽

Alfalfa Mosaic Virus ◽

Plant Viruses ◽

Yellow Mosaic Virus ◽

Tobacco Streak Virus ◽

Streak Virus

Multi-site sampling was conducted during 2011 and 2012 to assess the scope of virus disease problems of soybean in Ohio, USA. A total of 259 samples were collected from 80 soybean fields distributed in 42 Ohio counties, accounting for more than 90% of major soybean-growing counties in Ohio. A high-throughput RNA-Seq approach was adopted to identify all viruses in the samples that share sufficient sequence similarities with known plant viruses. To minimize sequencing costs, total RNA extracted from up to 20 samples were first pooled to make up regional pools, resulting in eight regional pools per year in both 2011 and 2012. These regional pools were further pooled into two yearly master pools of RNA, and sequenced using the Illumina's HiSeq2000 platform. Bioinformatic analyses of sequence reads led to the identification of signature sequences of nine different viruses. The originating locations of these viruses were then mapped with PCR or RT-PCR. This study confirmed the widespread distribution of Bean pod mottle virus, Soybean vein necrosis virus, Tobacco ringspot virus, and Tobacco streak virus in Ohio. It additionally revealed occasional association of Alfalfa mosaic virus, Bean yellow mosaic virus, Clover yellow vein virus, Soybean mosaic virus, and Soybean Putnam virus with Ohio soybean. This is the first statewide survey of soybean viruses in Ohio, and provides the much-needed baseline information for management of virus diseases of soybean. Accepted for publication 20 May 2016. Published 10 June 2016.

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Occurrence and Relative Incidence of Viruses Infecting Soybeans in Iran

Plant Disease ◽

10.1094/pdis.2004.88.10.1069 ◽

2004 ◽

Vol 88 (10) ◽

pp. 1069-1074 ◽

Cited By ~ 28

Author(s):

A. R. Golnaraghi ◽

N. Shahraeen ◽

R. Pourrahim ◽

Sh. Farzadfar ◽

A. Ghasemi

Keyword(s):

Mosaic Virus ◽

Soybean Mosaic Virus ◽

Alfalfa Mosaic Virus ◽

Soybean Seed ◽

Ringspot Virus ◽

Yellow Mosaic Virus ◽

Tobacco Streak Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Streak Virus ◽

Natural Occurrence

A survey was conducted to determine the incidence of Alfalfa mosaic virus (AlMV), Bean common mosaic virus (BCMV), Bean yellow mosaic virus (BYMV), Blackeye cowpea mosaic virus (BlCMV), Cucumber mosaic virus (CMV), Pea enation mosaic virus (PEMV), Peanut mottle virus (PeMoV), Soybean mosaic virus (SMV), Tobacco mosaic virus (TMV), Tobacco ringspot virus (TRSV), Tobacco streak virus (TSV), Tomato ringspot virus (ToRSV), and Tomato spotted wilt virus (TSWV) on soybean (Glycine max) in Iran. Totals of 3,110 random and 1,225 symptomatic leaf samples were collected during the summers of 1999 and 2000 in five provinces of Iran, where commercial soybean is grown, and tested by enzyme-linked immunosorbent assay (ELISA) using specific polyclonal antibodies. Serological diagnoses were confirmed by electron microscopy and host range studies. The highest virus incidence among the surveyed provinces was recorded in Mazandaran (18.6%), followed by Golestan (15.7%), Khuzestan (14.2%), Ardabil (13.9%), and Lorestan (13.5%). Incidence of viruses in decreasing order was SMV (13.3%), TSWV (5.4%), TRSV (4.2%), TSV (4.1%), PEMV (2.9%), BYMV (2.2%), ToRSV (2.1%), AlMV (1.3%), BCMV (0.8%), and CMV (0.6%). Additionally, 1.5% of collected leaf samples had positive reactions in ELISA with antiserum to TMV, indicating the possible infection of soybeans in Iran with a Tobamovirus that is related serologically to TMV. Of 195 leaves from plants showing soybean pod set failure syndrome (PSF) in Mazandaran and Lorestan, only 14 (7.2%) samples had viral infection. No correlation was observed between PSF and presence of the 13 viruses tested, suggesting the involvement of other viruses or factors in this syndrome. To investigate the presence of seed-borne viruses, including SMV, TRSV, ToRSV, and TSV, 7,830 soybean seeds were collected randomly at harvesting time from the major sites of soybean seed production located in Mazandaran and Golestan provinces. According to ELISA analyses of germinated seedlings, 7.1 and 8.9% of the seed samples from Golestan and Mazandaran provinces, respectively, transmitted either SMV, TRSV, ToRSV, or TSV through seed. We also showed that SMV and other seed transmissible viruses, as well as TSWV, usually are the most prevalent viruses in soybean fields in Iran. In this survey, natural occurrence of AlMV, BCMV, BlCMV, BYMV, CMV, PEMV, PeMoV, and TSWV was reported for the first time on soybeans in Iran.

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Ilarviruses of Prunus spp.: A Continued Concern for Fruit Trees

Phytopathology ◽

10.1094/phyto-02-12-0023-rvw ◽

2012 ◽

Vol 102 (12) ◽

pp. 1108-1120 ◽

Cited By ~ 52

Author(s):

V. Pallas ◽

F. Aparicio ◽

M. C. Herranz ◽

K. Amari ◽

M. A. Sanchez-Pina ◽

...

Keyword(s):

Mosaic Virus ◽

Genome Organization ◽

Alfalfa Mosaic Virus ◽

Fruit Trees ◽

Plant Viruses ◽

International Committee ◽

Economic Losses ◽

Tobacco Streak Virus ◽

Streak Virus ◽

Prunus Spp

Prunus spp. are affected by a large number of viruses, causing significant economic losses through either direct or indirect damage, which results in reduced yield and fruit quality. Among these viruses, members of the genus Ilarvirus (isometric labile ringspot viruses) occupy a significant position due to their distribution worldwide. Although symptoms caused by these types of viruses were reported early in the last century, their molecular characterization was not achieved until the 1990s, much later than for other agronomically relevant viruses. This was mainly due to the characteristic liability of virus particles in tissue extracts. In addition, ilarviruses, together with Alfalfa mosaic virus, are unique among plant viruses in that they require a few molecules of the coat protein in the inoculum in order to be infectious, a phenomenon known as genome activation. Another factor that has made the study of this group of viruses difficult is that infectious clones have been obtained only for the type member of the genus, Tobacco streak virus. Four ilarviruses, Prunus necrotic ringspot virus, Prune dwarf virus, Apple mosaic virus, and American plum line pattern virus, are pathogens of the main cultivated fruit trees. As stated in the 9th Report of the International Committee on Taxonomy of Viruses, virions of this genus are “unpromising subjects for the raising of good antisera.” With the advent of molecular approaches for their detection and characterization, it has been possible to get a more precise view of their prevalence and genome organization. This review updates our knowledge on the incidence, genome organization and expression, genetic diversity, modes of transmission, and diagnosis, as well as control of this peculiar group of viruses affecting fruit trees.

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Leafroll Virus Is Common in Cultivated American Grapevines in Western New York

Plant Disease ◽

10.1094/pdis.1998.82.9.1062c ◽

1998 ◽

Vol 82 (9) ◽

pp. 1062-1062 ◽

Cited By ~ 4

Author(s):

W. F. Wilcox ◽

Z.-Y. Jiang ◽

D. Gonsalves

Keyword(s):

New York ◽

Fruit Set ◽

Chenopodium Quinoa ◽

Tobacco Streak Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Mechanical Transmission ◽

Streak Virus ◽

Production Region ◽

The Individual ◽

Leafroll Virus

American grapevines (Vitis labrusca L. ‘Niagara’; Vitis × labruscana L. H. Bailey ‘Concord’ and ‘Catawba’; V. labrusca × V. riparia Michx. ‘Elvira’) from 24 vineyards in the New York portion of the Lake Erie production region (>13,000 ha cultivated) were tested to explore a possible relationship between virus infection and an unexplained fruit set malady in the district. One-year-old cane segments were collected 4 to 6 weeks before budbreak from 65 individual vines, which previously had been identified as malady positive or negative. Preparations from bark scrapings were tested for the presence of double-stranded (ds) RNA and for fan leaf degeneration virus, tobacco streak virus, and grapevine leafroll associated closterovirus-3 (GLRaV-3) by enzyme-linked immunosorbent assay (ELISA). Mechanical transmission of other potential viruses to Chenopodium quinoa was attempted with sap extracted from young shoots forced from intact segments of sampled canes. GLRaV-3 was detected in 17 (26%) of the sampled vines from eight (33%) of the vineyards, but there was no apparent relationship between infected vines and the fruit set malady. Vines of all four cultivars were infected. dsRNA was detected in all 17 samples positive for GLRaV-3 plus four additional samples. No other viruses were detected. Near harvest, nine vines (from two vineyards) previously testing positive for GLRaV-3 were examined and retested; all nine tested positive again, although none showed any overt symptoms of viral infection. This is believed to be the first report of GLRaV-3 from American grape vineyards in New York. The source of these infections is unknown: all vines were self rooted, the individual vineyards had been planted independently at different times, and V. vinifera and its hybrids are rare in the district. Wild grapevines (primarily V. riparia) are abundant in the region, although it has been reported that leafroll disease does not occur naturally in wild North American grapes (1). Nevertheless, our results indicate that cultivated American grapevines can be common reservoirs of GLRaV-3, and furthermore suggest the need to reassess the possibility that wild grapes also may serve as reservoirs of the virus. Trials are currently underway to determine possible effects of GLRaV-3 on cv. Concord, the most widely planted variety in the region. Reference: (1) A. C. Goheen. 1988. Leafroll. Page 52 in: Compendium of Grape Diseases. R. C. Pearson and A. C. Goheen, eds. American Phytopathological Society, St. Paul, MN.

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Prevalence and Molecular Characterization Coat Protein Gene of Tobacco streak virus Causing Peanut Stem Necrosis Disease in Coastal and Rayalaseema Districts of Andhra Pradesh, South-India

Legume Research - An International Journal ◽

10.18805/lr-4515 ◽

2021 ◽

Author(s):

K. Saratbabu ◽

K. Vemana ◽

A.K. Patibanda ◽

B. Sreekanth ◽

V. Srinivasa Rao

Keyword(s):

Coat Protein ◽

Molecular Characterization ◽

Andhra Pradesh ◽

Disease Incidence ◽

Tobacco Streak Virus ◽

Enzyme Linked Immunosorbent Assay ◽

Streak Virus ◽

Rt Pcr ◽

Cp Gene ◽

Stem Necrosis

Background: Peanut stem necrosis disease (PSND) caused by Tobacco streak virus (TSV) is a major constraint for groundnut production in Andhra Pradesh (A.P.). However, studies on prevalence and spread of the disease confined to only few districts of A.P. with this background current study focused on incidence and spread of the disease in entire state of A.P. Further an isolate of TSV occurring in A.P. characterized on the basis of genetic features by comparing with other TSV isolates originated from different hosts and locations from world.Methods: Roving survey was conducted during kharif 2017-18 in groundnut growing districts of Andhra Pradesh (A.P.) for peanut stem necrosis disease incidence. Groundnut plants showing PSND symptoms were collected and tested with direct antigen coating enzyme linked immunosorbent assay (DAC-ELISA). Groundnut samples found positive by ELISA once again tested by reverse transcription polymerase chain reaction (RT-PCR). The representative TSV-GN-INDVP groundnut isolate from Prakasham district was maintained on cowpea seedlings by standard sap inoculation method in glasshouse for further molecular characterization. The Phylogenetic tree for coat protein (CP) gene was constructed using aligned sequences with 1000 bootstrap replicates following neighbor-joining phylogeny.Result: Thirty-eight (52.7%) of seventy-two groundnut samples collected from different locations in A.P were given positive reaction to TSV by DAC-ELISA. For the first time, PSND incidence observed in coastal districts (Krishna, Guntur, Sri Pottisriramulu Nellore, Prakasham) of A.P. Maximum PSND incidence recorded from Bathalapalli (22.2%) and the minimum incidence in Mulakalacheruvu (4.1%). The coat protein (CP) gene of TSV-GN-INDVP groundnut isolate was amplified by RT-PCR and it shared maximum per cent nucleotide identity (97.51-98.62%) with TSV isolates from groundnut and other different crops reported in India. All Indian isolates cluster together irrespective of crop and location based on the phylogenetic analysis.

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